28 Jobs für Clinical Trials Assistant
Stellenangebote Clinical Trials Assistant Jobs
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-[. .. ] efficiency Preparation and review of study documentation and feasibility studies for new proposals Potential to assist in training and mentoring fellow CRAs You are: 18 months of experience in clinical trials Degree in medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability [. .. ]
Job am 14.01.2026 bei Jooble gefunden
FERCHAU GmbH
Clinical Trials Assistant, Clinical Trials
• Biberach an der Riß
Mitarbeiterevents
Als
Clinical Trial Administrator:in unterstützt du spannende, internationale Studienprojekte. Bei uns hast du die Möglichkeit, aktiv an innovativen medizinischen Lösungen mitzuwirken und in einem Umfeld zu arbeiten, das deine Entwicklung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fördert. Unterstützung von Trial Managern für das eigenständige Management des CTSU-Studienteams innerhalb der Matrixstruktur Planung, Steuerung und Kontrolle von Zeitplänen, Kosten [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
Homeoffice möglich
[. .. ] internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer the exciting opportunity to join the FSP [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team as Experienced Clinical Trials Assistant (m/w/d) in full-time and work in a combination of office and home-office preferable in the Hamburg area. RESPONSIBILITIES Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) [. .. ]
Job gestern bei Neuvoo gefunden
IQVIA
Experienced Clinical Trial Coordinator (m/w/d) , Home Office
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] science, the medical or pharmaceutical field or office management. At least 2-4 years experience as Clinical Trial Coordinator or within another administrative role in clinical research, e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. as Clinical Trials Assistant, Study Start-Up Assistant. Knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes [. .. ]
Job am 14.01.2026 bei Jooble gefunden
FERCHAU GmbH
• Biberach an der Riß
Mitarbeiterevents
Als
Clinical Trial Administrator:in unterstützt du spannende, internationale Studienprojekte. Bei uns hast du die Möglichkeit, aktiv an innovativen medizinischen Lösungen mitzuwirken und in einem Umfeld zu arbeiten, das deine Entwicklung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fördert. Unterstützung von Trial Managern für das eigenständige Management des CTSU-Studienteams innerhalb der Matrixstruktur Planung, Steuerung und Kontrolle von Zeitplänen, Kosten [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• München
This is what you will do: The
Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active participant in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Clinical Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner on a site level. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure delivery and [. .. ] Sees change as an opportunity to improve performance and add value to the business. Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time. Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. Proactivity and assertively when communicating with internal stakeholders and sites Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/ [. .. ]
Job gestern bei Jooble gefunden
Fraunhofer- Gesellschaft
• Aachen
Work-Life-Balance
[. .. ] are Europe s leading center for contract research and development. In our Laser Medical Technology and Biophotonics department, we develop innovative laser surgical procedures and systems in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaboration with leading clinical partners and medical technology companies. We are looking for a committed medical physicist/ physicist to join our laser surgery projects as soon as possible. The ideal candidate will enjoy interdisciplinary collaboration and be willing to take on responsibility in challenging research and development projects in the field of robotic laser [. .. ] laser technology, and information technology You will implement the developed processes together with our engineers and technicians, continuously expanding your knowledge in the process In addition, you will conduct field trials in a clinical environment to test the developed methods and devices under realistic conditions What you contribute You have an excellent master s degree in medical physics, physics, or related fields and have in-depth knowledge of optics and laser technology Ideally, you have anatomical knowledge and programming experience in [. .. ]
Job gestern bei Jooble gefunden
Fraunhofer- Gesellschaft
Research assistant in the field of electrical engineering/ computer engineering
• Aachen
Work-Life-Balance
[. .. ] of laser technology for 40 years and are Europe s leading center for contract research and development. In our Laser Medical Technology and Biophotonics department, we work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together with leading clinical partners and medical technology companies to develop innovative laser surgical procedures and systems. For our projects in the field of laser surgery, we are looking for an engineer specialized in electrical engineering, computer engineering, or computational science to start as soon as possible. Requirements include enjoyment of interdisciplinary collaboration and [. .. ] use in clinical settings. Your development work will focus on automated mechatronic systems for minimally invasive applications in neurosurgery, maxillofacial surgery, and spinal surgery. In addition, you will conduct field trials in a clinical environment to test the developed methods and devices under realistic conditions You will work closely with clinical and industrial partners from the fields of medical technology, laser technology, and information technology, allowing you to continuously expand your knowledge What you contribute You have an excellent master s [. .. ]
Job vor 7 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
• Baden- Wurttemberg
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description
Assistant CRA-Germany 2 Year Fixed Term contract At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on a global scale. Join our colleagues in bringing our Mission to life-enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Assistant CRA (m/f/d)
• Karlsruhe
Work Schedule Standard (Mon-Fri) Environmental Conditions Office
Assistant CRA-Germany 2 Year Fixed Term contract At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global scale. Join our colleagues in bringing our Mission to life-enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Massive Bio, Inc.
• Deutschland
About Massive Bio Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by eliminating the barriers of geography, financial constraints, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] contact strategy, relationship development, and post-enrollment support. Track outcomes against enrollment and revenue KPIs, and share structured recommendations that improve quality and performance over time. Bachelors degree required (Physician Assistant, Business Administration, or a related field preferred) . Strong project and stakeholder management skills, with the ability to manage multiple events and priorities simultaneously. Advanced English required. 76095068 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Massive Bio, Inc.
Provider Engagement Partnerships Manager-Germany (Oncology)
• Deutschland
About Massive Bio Every cancer patient deserves access to treatment options. Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] eliminating the barriers of geography, financial constraints, and information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] Collaborate cross-functionally with Clinical Operations, Marketing, and Product to tailor approaches for key accounts and ensure alignment with customer needs and local dynamics. Qualifications Requirements Bachelors degree required (Physician Assistant, Business Administration, or a related field preferred) . 3+ years of experience in sales, business development, provider engagement, account-facing roles, or similar commercial responsibilities, ideally within healthcare, pharma, oncology, or clinical trials. Demonstrated ability to build and leverage a physician network and drive measurable engagement (e. g. , attendance, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Massive Bio, Inc.
• Deutschland
About Massive Bio Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by eliminating the barriers of geography, financial constraints, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] contact strategy, relationship development, and post-enrollment support. Track outcomes against enrollment and revenue KPIs, and share structured recommendations that improve quality and performance over time. Bachelors degree required (Physician Assistant, Business Administration, or a related field preferred) . Strong project and stakeholder management skills, with the ability to manage multiple events and priorities simultaneously. Advanced English required. 76095071 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Massive Bio, Inc.
Client Success Support Manager (m/w/d)
• Deutschland
About Massive Bio Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by eliminating the barriers of geography, financial constraints, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] contact strategy, relationship development, and post-enrollment support. Track outcomes against enrollment and revenue KPIs, and share structured recommendations that improve quality and performance over time. Bachelors degree required (Physician Assistant, Business Administration, or a related field preferred) . Strong project and stakeholder management skills, with the ability to manage multiple events and priorities simultaneously. Advanced English required. 76095070 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
CRA Assistant (m/w/d)
• Karlsruhe
Assistant CRA-Germany At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. We provide our teams with the resources needed to achieve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. We offer continued [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Massive Bio, Inc.
Client Support Executive
• Deutschland
About Massive Bio Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by eliminating the barriers of geography, financial constraints, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] contact strategy, relationship development, and post-enrollment support. Track outcomes against enrollment and revenue KPIs, and share structured recommendations that improve quality and performance over time. Bachelors degree required (Physician Assistant, Business Administration, or a related field preferred) . Strong project and stakeholder management skills, with the ability to manage multiple events and priorities simultaneously. Advanced English required. 76095069 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Global Trial Associate (GTA) - Global Clinical Operations Leadership Development Program 2026
• Neuss, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https:/ / Job Function Job Function: R D Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Job Sub Function: Clinical Trial Support Job Category: Professional All Job Posting Locations: Beerse, Antwerp, Belgium, Breda, Netherlands, Copenhagen, Istanbul, Turkey, Madrid, Spain, Neuss, North Rhine-Westphalia, Germany, Paris, le-de-France, France, Prague, Czechia, Solna, Stockholm County, Sweden, Warsaw, Masovian, Poland Job Description The GCO Leadership Development Program consists of 12 months of [. .. ] of pharmaceutical development, GCO standard operation procedures, policies and regulatory requirements, logistical and administrative tasks related to trial management (start-up, execution and closing phases) and patient safety in clinical trials. The GTA will gain knowledge of and support activities of the Site Manager (SM) and Local Trial Manager (LTM) positions under the direct supervision of LTM and SM mentors, Program Manager, and/or Functional Manager (FM) . Upon successful completion of the program, GTAs will be placed in either the LTM or SM role depending on business need and skill set of the GTAs. Responsibilities Provide administrative and logistical support to Clinical Trial Assistant (CTAs) , SM and/or LTM in tracking progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence, materials, drug distribution and other relevant tasks as appropriate in adherence to relevant SOPs, policies, and local regulatory requirements. Support the local study team in performing site feasibility [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Director Clinical Operations
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Select how often (in days) to receive an alert: Mainz, Germany; London, United Kingdom full time Job ID:9757 About the Role: As Director
Clinical Operations, you will lead clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trial teams to ensure compliance with regulatory standards and drive successful study execution. Your leadership will be pivotal in resource planning, team development, and strategic decision-making to support Bio NTechs delivery of high-quality oncology programs. You will collaborate within a dynamic environment that values [. .. ] and Associate Directors Clinical Trial Management Plan resources for the team in alignment with Senior Director, Clinical Operations Govern CROs and vendors while contributing to strategic sourcing decisions for clinical trials A Good Match: University degree or experience in a medical profession (e. g. , Nurse or Medical Technical Assistant) Profound knowledge of relevant legislation and international guidelines (ICH-GCP) for clinical research projects 12+ years of experience in project management, regulatory submissions, and global study organizations, including 6+ years leading global clinical development teams Proficiency in software tools such as Word, Excel, Power Point, MS Project Strong organizational and [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Anesthesia Tech/ CNA
• Berlin
[. .. ] from the beach, Tidal Health offers the widest array of specialty and subspecialty services such as neurosurgery, cardiothoracic surgery, joint replacement, emergency/ trauma care, comprehensive cancer care, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] wound care and clinical trials and research. Take advantage of our tuition assistance and scholarship programs to grow both personally and professionally. Anesthesia Tech/ CNA Position Summary The Anesthesia Tech/ CNA is responsible for assisting licensed anesthesia providers in the acquisition, preparation and application of the equipment and supplies required for the administration of anesthesia. [. .. ] before, during, and after anesthesia. The Tech will function as patient transporter when not completing anesthesia duties. Anesthesia Tech/ CNA Position Requirements High School graduate or equivalent. Active Certified Nursing Assistant (C. N. A. ) license in the state of Maryland required. Experience Minimum one (1) year experience in hospital or related area, preferably in Surgical Services. Anesthesia Tech/ CNA Work Schedule Monday Friday, primarily day shift. At Tidal Health, full-time employees working at least 72 hours per pay period, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Assistant pro Jahr?
Als Clinical Trials Assistant verdient man zwischen EUR 35.000,- bis EUR 50.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Assistant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 28 offene Stellenanzeigen für Clinical Trials Assistant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Assistant Jobs?
Aktuell suchen 9 Unternehmen nach Bewerbern für Clinical Trials Assistant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Assistant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Assistant Stellenangebote:
- Abb Vie (6 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- FERCHAU GmbH (2 Jobs)
- IQVIA (2 Jobs)
- Fraunhofer- Gesellschaft (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Assistant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Assistant Jobs werden derzeit in Rheinland-Pfalz (2 Jobs), Hessen (1 Jobs) und Sachsen-Anhalt (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Assistant Jobs?
Clinical Trials Assistant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
